Reaction Details |
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Target | Carbonic anhydrase 15 |
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Ligand | BDBM50296250 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_579804 (CHEMBL1059705) |
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IC50 | 93100±n/a nM |
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Citation | Parkkila, S; Innocenti, A; Kallio, H; Hilvo, M; Scozzafava, A; Supuran, CT The protein tyrosine kinase inhibitors imatinib and nilotinib strongly inhibit several mammalian alpha-carbonic anhydrase isoforms. Bioorg Med Chem Lett19:4102-6 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 15 |
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Name: | Carbonic anhydrase 15 |
Synonyms: | CAH15_MOUSE | Ca15 | Car15 |
Type: | PROTEIN |
Mol. Mass.: | 35484.02 |
Organism: | Mus musculus |
Description: | ChEMBL_651955 |
Residue: | 324 |
Sequence: | MWALDFLLSFLLIQLAAQVDSSGTWCYDSQDPKCGPAHWKELAPACGGPTQSPINIDLRL
VQRDYTLKPFIFQGYDSAPQDPWVLENDGHTVLLRVNSCQQNCPAIRGAGLPSPEYRLLQ
LHFHWGSPGHQGSEHSLDEKHGSMEMHMVHMNTKYQSMEDARSQPDGFAILAVLLVEEDR
DNTNFSAIVSGLKNLSSPGVAVNLTSTFALASLLPSALRLLRYYRYSGSLTTPGCEPAVL
WTVFENTVPIGHAQVVQFQAVLQTGPPGLHPRPLTSNFRPQQPLGGRRISASPEASVRSS
VSTLPCLHLALVGLGVGLRLWQGP
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BDBM50296250 |
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n/a |
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Name | BDBM50296250 |
Synonyms: | (S,Z)-3-(2-hydroxy-5-(1-hydroxy-3-methylbutyl)-4-methoxyphenyl)acrylate | CHEMBL560175 |
Type | Small organic molecule |
Emp. Form. | C15H20O5 |
Mol. Mass. | 280.3163 |
SMILES | COc1cc(O)c(\C=C/C(O)=O)cc1[C@@H](O)CC(C)C |r| |
Structure |
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